Table of Contents
Main Features
Eye Findings
Other Findings
Etiology
Resources
Kabuki Syndrome
Main Features
Distinctive facial features
long palpebral fissures with eversion of the lateral 1/3 of lower eyelid
arched and broad eyebrows often with sparsness laterally
short columella with depressed nasal tip
large prominent cupped ears
From reference [4]
developmental delay and intellectual disability
Post natal growth deficiency
Skeletal anomalies
Persistent fetal fingertip pads
Eye Findings
Everted lower eyelids
Found in about 1/3
Strabismus
Ptosis
Blue sclerae
Coloboma
Marcus Gunn jaw wink
Peters anomaly
More Rare
Optic nerve hypoplasia
colobomatous microphthalmia
anophthalmia
Other Findings
Congenital heart defects
GU anomalies
Cleft palate
Increased susceptibility to infections and autoimmune disorders
Immune thrombocytopenia
Etiology
75% from KMT2D gene mutations (autosomal dominant)
8% from KDM6A gene mutations (X-linked dominant)
rest unknown
Resources
Adam MP et al. Kabuki Syndrome: International Consensus Diagnostic Criteria. Journal of Medical Genetics. 2019;56(2):89-95.
Adam MP et al. Kubuki Syndrome. GeneReviews
Panneerselvam S. et al. Oculoplastic Operative Considerations for Kabuki Syndrome: A Case Report and Review of the Literature. Ophthalmic Plast Reconstr Surg. 2025;41(3):e104-e106.
Li, Yun et al (2011). A mutation screen in patients with Kabuki syndrome. Human Genetics. 2011;130:715-24.
syndrome